150771-44-1 Usage
Description
2H-Hexafluoroisopropyl allyl ether, with a minimum purity of 97%, is a chemical compound characterized by its unique structure with six fluorine atoms and an allyl functional group. 2H-HEXAFLUOROISOPROPYL ALLYL ETHER, 97% MIN. is known for its stability, resistance to heat and chemicals, and distinctive reactivity and properties, making it a valuable asset for researchers and industrial users in the field of organic chemistry.
Uses
Used in Organic Synthesis:
2H-Hexafluoroisopropyl allyl ether, 97% MIN., is used as a reagent and solvent in organic synthesis for its unique reactivity and properties. Its stability and resistance to heat and chemicals make it suitable for various laboratory applications.
Used in Research and Development:
Due to its high purity and distinctive properties, 2H-hexafluoroisopropyl allyl ether, 97% MIN., is utilized in research and development for the exploration of new chemical reactions and the synthesis of novel compounds in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 150771-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 150771-44:
(8*1)+(7*5)+(6*0)+(5*7)+(4*7)+(3*1)+(2*4)+(1*4)=121
121 % 10 = 1
So 150771-44-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6F6O/c1-3(2-13)4(5(7,8)9)6(10,11)12/h4,13H,1-2H2
150771-44-1Relevant articles and documents
Rate and product studies on the solvolyses of allyl chloroformate
Koh, Han Joong,Kang, Suk Jin
, p. 4117 - 4121 (2013/08/23)
The solvolysis rate constants of allyl chloroformate (CH 2=CHCH2OCOCl, 3) in 30 different solvents are well correlated with the extended Grunwald-Winstein equation, using the NT solvent nucleophilicity scale and YCl solvent ionizing scale, with the sensitivity values of 0.93 ± 0.05 and 0.41 ± 0.02 for l and m, respectively. These l and m values can be considered to support a S N2 reaction pathway. The activation enthalpies (ΔH≠) were 12.5 to 13.4 kcal·mol-1 and the activation entropies (ΔS≠) were -34.4 to -37.3 cal·mol-1·K -1, which is also consistent with the proposed bimolecular reaction mechanism. The solvent kinetic isotope effect (SKIE, kMeOH/k MeOD) of 2.16 was also in accord with the SN2 mechanism. The values of product selectivity (S) for the solvolyses of 3 in alcohol/water mixtures was 1.3 to 3.9, which is also consistent with the proposed bimolecular reaction mechanism.
